Canonical Allele Identifier: CA1883176794
Gene: RXRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134408215G= , CM000671.2:g.134408215G= GRCh38
NC_000009.11:g.137300061G= , CM000671.1:g.137300061G= GRCh37
NC_000009.10:g.136439882G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.346G= MANE Select ENSP00000419692.1:p.Val116=
ENST00000672570.1:c.265G= ENSP00000500402.1:p.Val89=
ENST00000356384.4:n.756G=
ENST00000481739.1:c.346G= ENSP00000419692.1:p.Val116=
NM_001291920.1:c.265G= NP_001278849.1:p.Val89=
NM_001291921.1:c.55G= NP_001278850.1:p.Val19=
NM_002957.5:c.346G= NP_002948.1:p.Val116=
NM_002957.6:c.346G= MANE Select NP_002948.1:p.Val116=
NM_001291921.2:c.55G= NP_001278850.1:p.Val19=
NM_001291920.2:c.265G= NP_001278849.1:p.Val89=